A curated catalogue of human genomic structural variation




Variant Details

Variant: essv12503613



Internal ID5764048
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:110914754..110919578hg38UCSC Ensembl
Innerchr6:110914792..110919540hg38UCSC Ensembl
Outerchr6:110914716..110919616hg38UCSC Ensembl
chr6:111235957..111240781hg19UCSC Ensembl
Innerchr6:111235995..111240743hg19UCSC Ensembl
Outerchr6:111235919..111240819hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg384825
hg194825
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3610370
Supporting Variants
SamplesNA19137
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv12503613
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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